US5935965AExpiredUtility

2- (2-Alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene!phenylacetic acid derivatives, their preparation and intermediate therefor, and use thereof

71
Assignee: BASF AGPriority: Nov 17, 1994Filed: Nov 7, 1995Granted: Aug 10, 1999
Est. expiryNov 17, 2014(expired)· nominal 20-yr term from priority
C07D 239/52C07D 239/30A01N 43/54C07D 239/56
71
PatentIndex Score
14
Cited by
32
References
13
Claims

Abstract

PCT No. PCT/EP95/04375 Sec. 371 Date May 6, 1997 Sec. 102(e) Date May 6, 1997 PCT Filed Nov. 7, 1995 PCT Pub. No. WO96/16047 PCT Pub. Date May 30, 19962-[(2-Alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene]-phenylacetic acid derivatives of the formula I where the index and the substituents have the following meanings: U is CH or N; V is O or NH; R is alkyl; R1 is cyano, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or phenyl; n is 0 or an integer from 1 to 4, processes and intermediates for their preparation, and their use are described.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A 2- (2-alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene!phenylacetic acid of the formula I ##STR11## where the index and the substituents have the following meanings: U is CH or N; V is O or NH;   R is C 1  -C6-alkyl;   R 1  is cyano, halogen, C 1  -C 4  -alkyl, C 1  -C 4  -haloalkyl, C 1  -C 4  -alkoxy, C 1  -C 4  -haloalkoxy or phenyl;   n is 0 or an integer from 1 to 4, where the radicals R 1  may be different if the value of n is greater than 1.   
     
     
       2. The phenylacetic acid of the formula I defined in claim 1, where U is CH and V is O. 
     
     
       3. The phenylacetic acid of the formula I defined in claim 1, where U is N and V is O. 
     
     
       4. The phenylacetic acid of the formula I defined in claim 1, where U is N and V is NH. 
     
     
       5. The phenylacetic acid of the formula I defined in claim 1, where R is methyl, ethyl, or iso-propyl. 
     
     
       6. The phenylacetic acid of the formula I defined in claim 5, where U is CH and V is O. 
     
     
       7. The phenylacetic acid of the formula I defined in claim 5, where U is N and V is O. 
     
     
       8. A composition suitable for controlling animal pests and harmful fungi, which comprises a solid or liquid carrier and a phenylacetic acid of the formula I as defined in claim 1. 
     
     
       9. A method for controlling animal pests and harmful fungi, which comprises treating the pests or harmful fungi or the materials, plants, soil or seed to be protected from them with an effective amount of a phenylacetic acid of the formula I as defined in claim 1. 
     
     
       10. A composition suitable for controlling animal pests and harmful fungi, which comprises a solid or liquid carrier and a phenylacetic acid of the formula I as defined in claim 5. 
     
     
       11. A method for controlling animal pests and harmful fungi, which comprises treating the pests or harmful fungi or the materials, plants, soil or seed to be protected from them with an effective amount of a phenylacetic acid of the formula I as defined in claim 5. 
     
     
       12. A sulfone of the formula IV ##STR12## where the index and the substituents have the following meanings: U is CH or N: V is O or NH:   R a  is C 1  -C 4  -alkyl;   R 1  is cyano, halogen, C 1  -C 4  -alkyl, C 1  -C 4  -haloalkyl, C 1  -C 4  -alkoxy, C 1  -C 4  -haloalkoxy or phenyl:   n is 0 or an integer from 1 to 4, where the radicals R 1  may be different if the value of n is greater than 1.   
     
     
       13. A process for preparing the phenylacetic acid of the formula I defined in claim 1, which comprises reacting a pyrimidin-4-ol of the formula II ##STR13## in an inert solvent in the presence of a base with a benzyl compound of the formula III ##STR14## where X is a nucleophilically replaceable leaving group.

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